A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218557



Internal ID22363860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22665606..22669897hg38UCSC Ensembl
chr10:22954535..22958826hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384292
hg194292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335366
SamplesHG00732
Known GenesPIP4K2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218557
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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